A case of children with primary intratesticular rhabdomyosarcoma

In children, the most typical soft tissue tumor is a rhabdomyosarcoma (RMS). A primary intratesticular rhabdomyosarcoma is quite uncommon. An eleven-year-old had a painless left testicular tumor for two months. The patient's left scrotum was found to have a firm, non-tender lump. A massive hypo...

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Autores principales: Majid, Ghani Ikhsan, Rachmadiyan, Alyadi, Octavian, Irvan, Karim, M. Ilhamul, Mardianty, Friska
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Oncology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720432/
https://www.ncbi.nlm.nih.gov/pubmed/36478963
http://dx.doi.org/10.1016/j.eucr.2022.102293
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author Majid, Ghani Ikhsan
Rachmadiyan, Alyadi
Octavian, Irvan
Karim, M. Ilhamul
Mardianty, Friska
author_facet Majid, Ghani Ikhsan
Rachmadiyan, Alyadi
Octavian, Irvan
Karim, M. Ilhamul
Mardianty, Friska
author_sort Majid, Ghani Ikhsan
collection PubMed
description In children, the most typical soft tissue tumor is a rhabdomyosarcoma (RMS). A primary intratesticular rhabdomyosarcoma is quite uncommon. An eleven-year-old had a painless left testicular tumor for two months. The patient's left scrotum was found to have a firm, non-tender lump. A massive hypoechoic intratesticular mass measuring 8.0 × 7.5 × 6.0 cm was found in the left scrotum by scrotal and abdominal ultrasonography. The patient had an inguinal orchiectomy. Histopathological examination disclosed botryoid rhabdomyosarcoma. Primary intratesticular rhabdomyosarcomas are rare. Radical orchiectomy and chemotherapy are recommended. It may increase overall and disease-free survival.
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spelling pubmed-97204322022-12-06 A case of children with primary intratesticular rhabdomyosarcoma Majid, Ghani Ikhsan Rachmadiyan, Alyadi Octavian, Irvan Karim, M. Ilhamul Mardianty, Friska Urol Case Rep Oncology In children, the most typical soft tissue tumor is a rhabdomyosarcoma (RMS). A primary intratesticular rhabdomyosarcoma is quite uncommon. An eleven-year-old had a painless left testicular tumor for two months. The patient's left scrotum was found to have a firm, non-tender lump. A massive hypoechoic intratesticular mass measuring 8.0 × 7.5 × 6.0 cm was found in the left scrotum by scrotal and abdominal ultrasonography. The patient had an inguinal orchiectomy. Histopathological examination disclosed botryoid rhabdomyosarcoma. Primary intratesticular rhabdomyosarcomas are rare. Radical orchiectomy and chemotherapy are recommended. It may increase overall and disease-free survival. Elsevier 2022-11-30 /pmc/articles/PMC9720432/ /pubmed/36478963 http://dx.doi.org/10.1016/j.eucr.2022.102293 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Oncology
Majid, Ghani Ikhsan
Rachmadiyan, Alyadi
Octavian, Irvan
Karim, M. Ilhamul
Mardianty, Friska
A case of children with primary intratesticular rhabdomyosarcoma
title A case of children with primary intratesticular rhabdomyosarcoma
title_full A case of children with primary intratesticular rhabdomyosarcoma
title_fullStr A case of children with primary intratesticular rhabdomyosarcoma
title_full_unstemmed A case of children with primary intratesticular rhabdomyosarcoma
title_short A case of children with primary intratesticular rhabdomyosarcoma
title_sort case of children with primary intratesticular rhabdomyosarcoma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720432/
https://www.ncbi.nlm.nih.gov/pubmed/36478963
http://dx.doi.org/10.1016/j.eucr.2022.102293
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